M. Pestana et P. Soaresdasilva, OUTFLOW OF DOPAMINE AND NORADRENALINE ORIGINATING FROM L-DOPA AND L-THREO-DOPS IN RAT RENAL TISSUES, General pharmacology, 25(5), 1994, pp. 879-885
1. The present study has examined the formation and outflow of newly-f
ormed dopamine (DA) and noradrenaline (NA) in slices of the renal cort
ex of rats given L-beta-3,4-dihydroxyphenylalanine (L-DOPA) (10, 30 or
100 mg/kg i.p.) and L-threo-3-(3,4-dihydroxyphenyl)serine (L-DOPS) (1
0, 30 or 100 mg/kg i.p.), respectively. The outflow of 3,4-dihydroxyph
enylacetic acid (DOPAC) and 3,4-dihydroxyphenylglycol (DOPEG), the dea
minated metabolites of DA and NA, respectively, was also measured. 2.
The accumulation of both newly-formed DA and DOPAC in renal tissues af
ter the administration of L-DOPA was found to be dose dependent; after
30 or 100 mg/kg L-DOPA, the levels of both DA and DOPAC were, respect
ively, 3- and 20-fold those observed after the administration of 10 mg
/kg L-DOPA. The outflow of DA and DOPAC in kidney slices of rats treat
ed with L-DOPA was found to progressively decline with time and reflec
ted the DA and DOPAC tissue contents. The rate constant (k)for DOPAC e
fflux (k = 0.0097) was higher (P < 0.01) than that for DA efflux (k =
0.0033) and did not depend on the dose of L-DOPA. DOPAC/DA perifusate
ratios were 2-fold those occurring in the tissues. 3. The levels of NA
in renal tissues of rats given 30 and 100 mg/kg L-DOPS were, respecti
vely, 3- and 6-fold those observed after the administration of 10 mg/k
g L-DOPS. The administration of L-DOPS was also found to be accompanie
d by the accumulation in renal tissues of DOPEG; this was, however, no
t dose dependent. 4. The outflow of NA progressively declined with tim
e and also reflected the tissue contents of NA; the outflow of DOPEG i
n the first collection period was found not to differ from those in su
bsequent collection periods. The rate constant for the loss of DOPEG (
k = 0.0483) was 10-fold that for the loss of NA (k = 0.038). The DOPEG
/NA ratio in the tissue was significantly lower than that in perifusat
e samples. In conclusion, the results presented here show that in cort
ical slices of the rat kidney a ranking order was obtained for the rat
e constants of efflux of k(DOPEG) much greater than k(DOPAC) > k(DA) =
k(NA) suggesting that the outflow of DA, NA, DOPAC and DOPEG formed i
n tubular epithelial cells depends on their relative lipophilicity, as
has been described in other cell types loaded with these catechol der
ivatives. These results also show that the amount of DA and NA which i
s leaving the compartment where the synthesis has occurred is a consta
nt source for deamination into, respectively, DOPAC and DOPEG.